Cyclosporin A and verapamil have different effects on energy metabolism in multidrug-resistant tumour cells

Br J Cancer. 1990 Jul;62(1):85-8. doi: 10.1038/bjc.1990.234.

Abstract

Cyclosporin A (Sandimmune) rapidly induced an increase in daunorubicin accumulation in multidrug-resistant human ovarian carcinoma cells (2780AD) and was more potent than verapamil. Steady-state 3H-cyclosporin A accumulation at 37 degrees C in 2780AD cells was 60-70% of that in the sensitive A2780 cells. A rapid increase of ATP consumption and lactate production was induced in 2780AD cells by verapamil, but not by cyclosporin A. These results suggest that the interactions of cyclosporin A and verapamil with P-glycoprotein, which leads to inhibition of drug transport, have a different mechanistic basis.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Monophosphate / analysis
  • Adenosine Triphosphate / analysis
  • Cell Line
  • Cyclosporins / pharmacology*
  • Daunorubicin / pharmacokinetics
  • Drug Resistance / physiology*
  • Energy Metabolism / drug effects*
  • Female
  • Humans
  • Lactates / biosynthesis
  • Lactic Acid
  • Ovarian Neoplasms / drug therapy
  • Ovarian Neoplasms / metabolism*
  • Verapamil / pharmacology*

Substances

  • Cyclosporins
  • Lactates
  • Lactic Acid
  • Adenosine Monophosphate
  • Adenosine Triphosphate
  • Verapamil
  • Daunorubicin